Canonical Allele Identifier: CA2067679645
Gene: HNF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120994322C= , CM000674.2:g.120994322C= GRCh38
NC_000012.11:g.121432125C= , CM000674.1:g.121432125C= GRCh37
NC_000012.10:g.119916508C= NCBI36
NG_011731.2:g.20577C= , LRG_522:g.20577C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000560968.6:c.750+122C= ENSP00000453965.2:n.750+122C=
ENST00000257555.11:c.872C= MANE Select ENSP00000257555.5:p.Pro291=
ENST00000257555.10:c.872C= ENSP00000257555.4:p.Pro291=
ENST00000400024.6:c.872C= ENSP00000476181.1:p.Pro291=
ENST00000402929.5:n.1007C=
ENST00000535955.5:n.43-3169C=
ENST00000538626.2:n.191-3169C=
ENST00000538646.5:c.685C= ENSP00000443964.1:p.Gln229=
ENST00000540108.1:c.*312C= ENSP00000445445.1:n.*312C=
ENST00000541395.5:c.872C= ENSP00000443112.1:p.Pro291=
ENST00000541924.5:c.713+616C= ENSP00000440361.1:n.713+616C=
ENST00000543427.5:c.633+696C= ENSP00000439721.2:n.633+696C=
ENST00000544413.2:c.872C= ENSP00000438804.1:p.Pro291=
ENST00000544574.5:c.73-2295C= ENSP00000438565.1:n.73-2295C=
ENST00000560968.5:c.893+122C=
ENST00000615446.4:c.-257-1940C= ENSP00000483994.1:n.-257-1940C=
ENST00000617366.4:c.586+743C= ENSP00000481967.1:n.586+743C=
NM_000545.5:c.872C= , LRG_522t1:c.872C= NP_000536.5:p.Pro291=
NM_000545.6:c.872C= NP_000536.5:p.Pro291=
NM_001306179.1:c.872C= NP_001293108.1:p.Pro291=
XM_005253931.2:c.872C= XP_005253988.1:p.Pro291=
XM_024449168.1:c.872C= XP_024304936.1:p.Pro291=
NM_000545.8:c.872C= MANE Select NP_000536.6:p.Pro291=
NM_001306179.2:c.872C= NP_001293108.2:p.Pro291=